Canonical Allele Identifier: CA891837062
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965312_87965313delinsGT , CM000672.2:g.87965312_87965313delinsGT GRCh38
NC_000010.10:g.89725069_89725070delinsGT , CM000672.1:g.89725069_89725070delinsGT GRCh37
NC_000010.9:g.89715049_89715050delinsGT NCBI36
NG_007466.2:g.106874_106875delinsGT , LRG_311:g.106874_106875delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1145_1146delinsGT ENSP00000514759.2:p.Val382Gly
ENST00000710265.1:c.*81_*82delinsGT ENSP00000518161.1:n.*81_*82delinsGT
ENST00000688158.2:n.1787_1788delinsGT
ENST00000688922.2:c.*882_*883delinsGT ENSP00000508742.2:n.*882_*883delinsGT
ENST00000700021.1:c.1007_1008delinsGT ENSP00000514757.1:p.Val336Gly
ENST00000700022.1:c.*391_*392delinsGT ENSP00000514758.1:n.*391_*392delinsGT
ENST00000700023.1:n.2210_2211delinsGT
ENST00000700024.1:n.2444_2445delinsGT
ENST00000706954.1:c.1052_1053delinsGT ENSP00000516674.1:p.Val351Gly
ENST00000706955.1:c.*1087_*1088delinsGT ENSP00000516675.1:n.*1087_*1088delinsGT
ENST00000686459.1:c.*638_*639delinsGT ENSP00000508909.1:n.*638_*639delinsGT
ENST00000688158.1:c.*1163_*1164delinsGT ENSP00000509254.1:n.*1163_*1164delinsGT
ENST00000688308.1:c.1052_1053delinsGT ENSP00000508752.1:p.Val351Gly
ENST00000688922.1:c.973_974delinsGT
ENST00000693560.1:c.1571_1572delinsGT ENSP00000509861.1:p.Val524Gly
ENST00000371953.8:c.1052_1053delinsGT MANE Select ENSP00000361021.3:p.Val351Gly
ENST00000371953.7:c.1052_1053delinsGT ENSP00000361021.3:p.Val351Gly
NM_000314.5:c.1052_1053delinsGT NP_000305.3:p.Val351Gly
NM_000314.6:c.1052_1053delinsGT NP_000305.3:p.Val351Gly
NM_001304717.2:c.1571_1572delinsGT NP_001291646.2:p.Val524Gly
NM_001304718.1:c.461_462delinsGT NP_001291647.1:p.Val154Gly
XM_006717926.2:c.1007_1008delinsGT XP_006717989.1:p.Val336Gly
XM_011539982.1:c.956_957delinsGT XP_011538284.1:p.Val319Gly
XR_945791.1:n.1622_1623delinsGT
NM_000314.7:c.1052_1053delinsGT NP_000305.3:p.Val351Gly
NM_001304717.5:c.1571_1572delinsGT NP_001291646.4:p.Val524Gly
NM_001304718.2:c.461_462delinsGT NP_001291647.1:p.Val154Gly
NM_000314.8:c.1052_1053delinsGT MANE Select NP_000305.3:p.Val351Gly